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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 1
2006 3
2007 1
2008 1
2010 4
2011 2
2012 6
2013 4
2014 3
2015 5
2016 2
2017 6
2018 3
2019 3
2020 6
2021 5
2022 6
2023 2
2024 0

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54 results

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Page 1
Inherited macrothrombocytopenias.
Rabbolini DJ, Morel-Kopp MC, Stevenson W, Ward CM. Rabbolini DJ, et al. Among authors: morel kopp mc. Semin Thromb Hemost. 2014 Oct;40(7):774-84. doi: 10.1055/s-0034-1387922. Epub 2014 Aug 31. Semin Thromb Hemost. 2014. PMID: 25173502
Spectrum of the mutations in Bernard-Soulier syndrome.
Savoia A, Kunishima S, De Rocco D, Zieger B, Rand ML, Pujol-Moix N, Caliskan U, Tokgoz H, Pecci A, Noris P, Srivastava A, Ward C, Morel-Kopp MC, Alessi MC, Bellucci S, Beurrier P, de Maistre E, Favier R, Hézard N, Hurtaud-Roux MF, Latger-Cannard V, Lavenu-Bombled C, Proulle V, Meunier S, Négrier C, Nurden A, Randrianaivo H, Fabris F, Platokouki H, Rosenberg N, HadjKacem B, Heller PG, Karimi M, Balduini CL, Pastore A, Lanza F. Savoia A, et al. Among authors: morel kopp mc. Hum Mutat. 2014 Sep;35(9):1033-45. doi: 10.1002/humu.22607. Epub 2014 Jul 15. Hum Mutat. 2014. PMID: 24934643 Review.
GFI1B variants associated with thrombocytopenia.
Rabbolini DJ, Morel-Kopp MC, Ward CM, Stevenson WS. Rabbolini DJ, et al. Among authors: morel kopp mc. Platelets. 2017 Jul;28(5):525-527. doi: 10.1080/09537104.2017.1317734. Epub 2017 Jun 5. Platelets. 2017. PMID: 28580815 No abstract available.
Building platelet phenotypes: Diaphanous-related formin 1 (DIAPH1)-related disorder.
Rabbolini D, Liang HPH, Morel-Kopp MC, Connor D, Whittaker S, Dunkley S, Donikian D, Kondo M, Chen W, Stevenson WS, Campbell H, Joseph J, Ward C, Brighton T, Chen VM; Sydney Platelet Group. Rabbolini D, et al. Among authors: morel kopp mc. Platelets. 2022 Apr 3;33(3):432-442. doi: 10.1080/09537104.2021.1937593. Epub 2021 Jul 5. Platelets. 2022. PMID: 34223798
Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis.
Ewans LJ, Minoche AE, Schofield D, Shrestha R, Puttick C, Zhu Y, Drew A, Gayevskiy V, Elakis G, Walsh C, Adès LC, Colley A, Ellaway C, Evans CA, Freckmann ML, Goodwin L, Hackett A, Kamien B, Kirk EP, Lipke M, Mowat D, Palmer E, Rajagopalan S, Ronan A, Sachdev R, Stevenson W, Turner A, Wilson M, Worgan L, Morel-Kopp MC, Field M, Buckley MF, Cowley MJ, Dinger ME, Roscioli T. Ewans LJ, et al. Among authors: morel kopp mc. Eur J Hum Genet. 2022 Oct;30(10):1121-1131. doi: 10.1038/s41431-022-01162-2. Epub 2022 Aug 15. Eur J Hum Genet. 2022. PMID: 35970915 Free PMC article.
54 results